- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03354481
Automatization of Counting Procedures in Children With Dyscalculia (PROCEDYS)
April 22, 2026 updated by: Hospices Civils de Lyon
Researchers in numerical cognition usually think that the greatest and most common difficulty in children suffering from dyscalculia is retrieval of arithmetic facts from long-term memory.
However, we have recently shown that retrieval might not be the optimum strategy in mental arithmetic.
In fact, expert adults would rather solve simple problems such as 3 + 2 by automated and unconscious procedures.
Therefore, we hypothesize that children with dyscalculia might not present deficit in retrieval but, instead, in counting procedure automatization.
The aim of the current project is to test this challenging position.
Through a longitudinal approach, we plan to precisely examine the behavior of children suffering from dyscalculia over a 3-year period.
Children will be aged between 8 to 11 years at the beginning of the study and we will precisely observe the evolution of their solution times when they solve simple addition problems involving one-digit numbers.
If children with dyscalculia still struggle with simple additions three years, their solution times plotted on the sum of the problems should still follow an exponential function.
Indeed, if counting is not automated, difficulties necessarily increase with the progression on the number line or the verbal sequence, hence the exponential function.
On the contrary, if counting procedures tend towards automatization, moves along a number line will progressively become as easy at the beginning of the line as at the end, hence the linear function.
Importantly, a retrieval model would predict exactly the inverse pattern because, according to this model, the linear function, which is unanimously considered as the hallmark of counting procedures, should progressively be replaced by a non-linear function through practice.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
3
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Bron, France
- Hôpital Femme Mère Enfant
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
8 years to 11 years (Child)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Age between 8 and 11 years old
- Having a dyscalculia as described in the DSM (Diagnostic and Statistical Manual) V
Exclusion Criteria:
- Presenting a global intellectual deficit
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Behavioral recording of arithmetic and associated information
The experiment will contain several behavioral tasks in which solving time and correct answer will be recorded.
The main one will be a computerized task on arithmetic facts.
There will also be three additional tasks as described below.
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The experiment will contain several tasks.
The main one will be a computerized task on arithmetic facts where participants will have to solve simple additions.
There will also be three additional tasks: a processing speed task where the participant will have to tell the orientation of an arrow as fast as possible, a visuo-spatial task where the participant will have to reproduce a tapping block sequence and an arithmetic task where the participant will try to solve a maximum of operations in a limited time.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Response times to solve an informatics task on simple arithmetic facts resolution
Time Frame: Inclusion
|
Time between the apparition of the stimuli and the answer.
The task contain only addition of one digit numbers
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Inclusion
|
|
Response times to solve an informatics task on simple arithmetic facts resolution
Time Frame: 12 months
|
Time between the apparition of the stimuli and the answer.
The task contain only addition
|
12 months
|
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Response times to solve an informatics task on simple arithmetic facts resolution
Time Frame: 24 months
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Time between the apparition of the stimuli and the answer.
The task contain only addition
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24 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of correct responses to solve the informatics task on simple arithmetic facts resolution
Time Frame: 0+ 12 + 24 months
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0+ 12 + 24 months
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|
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Result of the digit span memory task
Time Frame: 0 month
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0 month
|
|
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Processing speed in an informatics task on arrow orientation
Time Frame: 0 month
|
0 month
|
|
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Result of the Corsi block tapping test
Time Frame: 0 month
|
0 month
|
|
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Result of the Tempo Test Rekenen
Time Frame: 0 month
|
The Tempo Test Rekenen is used to evaluate arithmetical ability.
It consists in solving several operations in a limited time.
|
0 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Jeanne Bagnoud, Romain Mathieu, Jasinta Dewi, Sandrine Masson, Sibylle Gonzalez-Monge, Zumrut Kasikci and Catherine Thevenot. "An investigation of the possible causes of arithmetic difficulties in children with dyscalculia". L'Année psychologique. 2021;121(3):217-237. doi : 10.3917/anpsy1.213.0217.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 12, 2018
Primary Completion (Actual)
September 19, 2019
Study Completion (Actual)
September 19, 2019
Study Registration Dates
First Submitted
November 20, 2017
First Submitted That Met QC Criteria
November 27, 2017
First Posted (Actual)
November 28, 2017
Study Record Updates
Last Update Posted (Actual)
April 27, 2026
Last Update Submitted That Met QC Criteria
April 22, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 69HCL17_0651
- 2017-A03134-49 (Other Identifier: ANSM)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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